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CompletedNCT02546154Updated May 23, 2019

Time to Relapse of Iron Deficiency Anaemia After Standard Treatment With The Intravenous Iron (Monofer®)

An observational study in Iron Deficiency Anaemia, sponsored by Pharmacosmos UK Ltd. Completed at 1 site in United Kingdom. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2019-05-23.

Sponsored by Pharmacosmos UK Ltd · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
359
Ages
18 Years and older
Sex
All
01

Study summary

The objective is to monitor and quality assure the efficacy, including effects on quality of life, and safety of Monofer® in Chronic Kidney Disease and Inflammatory Bowel Disease patient populations when Monofer® is used according to the Monofer® label (Summary of Product Characteristics, SPC) in current clinical practice and where standard routines are being followed.

Read the detailed description

Intravenous (IV) iron is a well-tolerated and efficacious treatment of iron deficiency anaemia in conditions such as Chronic Kidney Disease (CKD) and Inflammatory Bowel Disease (IBD). Several studies in CKD and IBD patients have shown that IV iron is superior to oral iron, most likely explained by decreased uptake and poor compliance (due to gastrointestinal side-effects) when using oral iron.

The patented Iron Isomaltoside 1000 (Monofer®) has been developed to overcome the current limitations of IV iron drugs with regards to safety and convenience of use. The possibility to administer Monofer® at high single doses (up to 20 mg/kg) reduces the number of treatment visits needed for full iron correction, which is cost-effective, resource and time-sparing, and a reduced drug exposure frequency decreases the risk of side-effects such as infusion reactions.

The objective of the study is to monitor and quality assure the efficacy, including effects on quality of life, and safety of Monofer® in CKD and IBD patient populations when Monofer® is used according to the Monofer® label (Summary of Product Characteristics, SPC) in current clinical practice and where standard routines are being followed. The scientific rationale being to fulfill a need for systematic information/auditing on applied practice including both short and long-term experience with the use of IV iron in different hospital settings and in current clinical practice. The outcome will provide an evidence base for optimised treatment procedures in terms of safety and efficacy.

The total duration of the study per site is approximately 21 months, which includes a 6 months enrollment period, a prospective observation period of at least 12 months, and a period of maximum 3 months prior to the last blood test. Patients will only attend hospital visits planned as part of their standard treatment and they will receive treatment as a part of standard care and according to the doctor's discretion. The number of patient visits depends on the number of Monofer® treatment courses needed during the study period. Each patient can receive one or more treatment courses during 12 months after informed consent. The last blood test will be taken after the last Monofer® treatment course which might occur 13-15 months after informed consent. Study termination will occur once the 12 months observational period has been completed for all patients and the last blood test has been collected from the last Monofer® treated patient in the study. Each treatment course can consist of one or more Monofer® administrations. For each administration of Monofer® either intravenous infusion or injection can be used. Pre- and post-treatment blood tests according to standard treatment and quality of life assessments for fatigue symptoms (FACIT-Fatigue and IBD-F Scales) are a part of the Monofer® treatment course. Laboratory assessments, i.e. anaemia work-up/treatment evaluation, shall be a part of local standard practice. The protocol does not accept any additional samples outside current local standard practice to be taken.

Clinical data management will be performed in accordance with applicable standards and data cleaning procedures. The collected data will systematically be entered into an electronic case report form (eClinicalOS, myEDC, license by BioStata Aps Denmark). The sources of information are the relevant treatment and laboratory results obtained from patient records as well as the quality of life questionnaires for fatigue symptoms. The data will be evaluated by the Pharmacosmos Medical Affairs teams and an external Data Management vendor located in a country within the European Union.

02

Conditions studied

  • Iron Deficiency Anaemia

Keywords

  • Iron
  • Anaemia
  • Anaemia, Iron-Deficiency
  • Kidney Diseases
  • Inflammatory Bowel Diseases
  • Fatigue
03

In context

Anemia

1,733 studies on the registry are indexed under Anemia; 246 are open to participants now.

This study's enrollment of 359 is above the median of 200 across 326 observational studies indexed under Anemia.

Browse Anemia studies →

Lead sponsor

This is the only study on the registry with Pharmacosmos UK Ltd as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Patients ≥18 years of age diagnosed with iron deficiency anaemia as a consequence of CKD or IBD.

Inclusion criteria

  • Patients diagnosed with iron deficiency anaemia as a consequence of CKD or IBD (on the basis of local definition or clinical judgement), treated on the doctor's discretion with Monofer® as standard treatment according to current practice

Exclusion criteria

Exclusion Criteria:

  • Patients diagnosed with both CKD and IBD
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
359 participants (actual)
Patient registry
No

Groups and cohorts

  • CKD, iron deficiency anaemia

    10% Iron Isomaltoside 1000 administered intravenously to Chronic Kidney Disease patients in doses at the doctor's discretion for treatment of iron deficiency anaemia.

    Drug: 10% Iron Isomaltoside 1000

  • IBD, iron deficiency anaemia

    10% Iron Isomaltoside 1000 administered intravenously to Inflammatory Bowel Disease patients in doses at the doctor's discretion for treatment of iron deficiency anaemia.

    Drug: 10% Iron Isomaltoside 1000

Interventions

  • Drug10% Iron Isomaltoside 1000

    Standard clinical practice and following the Monofer® label (SPC)

    Also known as: Monofer®

06

What researchers measure

Primary outcomes

  1. Time to relapse of iron deficiency anaemia

    Time frame: From screening until 12 months

Secondary outcomes

  1. Change in scores for fatigue symptoms

    Time frame: Immediately before to earliest 4 weeks after each treatment course during 12 months

  2. Change in anaemia-related blood parameter levels (haemoglobin, iron parameters)

    Time frame: Immediately before to earliest 4 weeks after each treatment course during 12 months

  3. IV iron dose (total needed dose per treatment course)

    Time frame: From screening until 12 months

  4. Number and seriousness of Adverse Drug Reactions

    Time frame: From screening until 12 months

07

Study locations

1 site
  • Royal Devon and Exeter Hospital NHS Foundation Trust
    Exeter, EX2 5DW, United Kingdom
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References and documents

Publications

  • Kalra PA, Bhandari S, Spyridon M, Davison R, Lawman S, Mikhail A, Reaich D, Pritchard N, McCafferty K, Moore J. NIMO-CKD-UK: a real-world, observational study of iron isomaltoside in patients with iron deficiency anaemia and chronic kidney disease. BMC Nephrol. 2020 Dec 10;21(1):539. doi: 10.1186/s12882-020-02180-2. PubMed 33302891 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 23, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02546154
Lead sponsor
Pharmacosmos UK Ltd
Collaborators
BioStata
Responsible party
Sponsor
First posted
Sep 10, 2015
Start date
Jan 22, 2016
Primary completion
Dec 2018
Completion
Dec 2018
Last update
May 23, 2019

Study contacts

Sylvia Simon, PhD
study chair · Pharmacosmos A/S
Jason Moore, BMedSci, BMBS, FRCP
principal investigator · Royal Devon and Exeter Hospital NHS Foundation Trust

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2019. You cannot join it, but the record below documents what was studied.

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